Introducing ecodesign in silica sol-gel materials

被引:127
作者
Baccile, Niki [1 ]
Babonneau, Florence [1 ]
Thomas, Bejoy [1 ]
Coradin, Thibaud [1 ]
机构
[1] Univ Paris 06, UPMC, CNRS, Coll France,UMR 7574, F-75005 Paris, France
关键词
SUPERCRITICAL CARBON-DIOXIDE; MESOPOROUS MOLECULAR-SIEVES; NUCLEAR-MAGNETIC-RESONANCE; ONE-POT SYNTHESIS; RICE HULL ASH; TEMPERATURE IONIC LIQUIDS; GLYCOL-MODIFIED SILANES; SODIUM-SILICATE; DISSOLUTION KINETICS; TEMPLATING ROUTE;
D O I
10.1039/b911123a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Over the last decade, ecodesign has been introduced as a concept and a methodological framework to identify and improve sustainability in product development. In this context, the 12 principles of green chemistry provide suitable guidelines for the elaboration of molecules and materials in conditions that meet some ecodesign-related criteria. Sol-gel chemistry is an interesting domain to be examined in this perspective because it was early identified as an eco-friendly process compared to traditional routes to ceramics and glasses. Thus it is not surprising that many recent developments in sol-gel technology have, explicitly or not, addressed sustainability issues. In this review, we present an overview of these advances, focusing on the chemistry of silica. Starting from the typical reaction involving tetraethoxysilane hydrolysis and condensation in hydro-alcoholic media in the presence of inorganic catalysts, the current alternatives in terms of precursors, solvents, catalysts and activation sources are presented. As an example of hybrid materials, the synthesis of surfactant-based mesostructured silica is commented. Manufacturing methods to nanoproducts, including sol-gel technology are also discussed in terms of sustainability. Finally, the recyclability and degradation of sol-gel silica are briefly commented on. As a conclusion, some perspectives and current limitations for the development of a "greener" sol-gel chemistry are provided, extending the discussion to non-silica materials.
引用
收藏
页码:8537 / 8559
页数:23
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